CN1096428C - Method of fabricating dispersion mobile optical fiber with smooth annular ring refractive index profile - Google Patents
Method of fabricating dispersion mobile optical fiber with smooth annular ring refractive index profile Download PDFInfo
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- 239000013307 optical fiber Substances 0.000 title claims abstract description 33
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 30
- 239000006185 dispersion Substances 0.000 title claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 94
- 238000000034 method Methods 0.000 claims abstract description 46
- 238000000151 deposition Methods 0.000 claims abstract description 19
- 238000010438 heat treatment Methods 0.000 claims abstract description 11
- 229910003902 SiCl 4 Inorganic materials 0.000 claims description 20
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 claims description 16
- 230000008021 deposition Effects 0.000 claims description 15
- 238000005530 etching Methods 0.000 claims description 5
- 239000000377 silicon dioxide Substances 0.000 claims 36
- 238000009833 condensation Methods 0.000 claims 3
- 230000005494 condensation Effects 0.000 claims 3
- 238000010304 firing Methods 0.000 claims 3
- 238000011946 reduction process Methods 0.000 claims 3
- 239000010453 quartz Substances 0.000 abstract description 22
- 239000000463 material Substances 0.000 abstract description 10
- 239000002994 raw material Substances 0.000 abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 4
- 239000001257 hydrogen Substances 0.000 abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 4
- 239000001301 oxygen Substances 0.000 abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 abstract description 4
- 238000007789 sealing Methods 0.000 abstract description 3
- 238000009826 distribution Methods 0.000 description 15
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 8
- 229910006113 GeCl4 Inorganic materials 0.000 description 5
- 229910003910 SiCl4 Inorganic materials 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- FDNAPBUWERUEDA-UHFFFAOYSA-N silicon tetrachloride Chemical compound Cl[Si](Cl)(Cl)Cl FDNAPBUWERUEDA-UHFFFAOYSA-N 0.000 description 5
- IEXRMSFAVATTJX-UHFFFAOYSA-N tetrachlorogermane Chemical compound Cl[Ge](Cl)(Cl)Cl IEXRMSFAVATTJX-UHFFFAOYSA-N 0.000 description 5
- 229910019213 POCl3 Inorganic materials 0.000 description 4
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium dioxide Chemical compound O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 4
- 229910005793 GeO 2 Inorganic materials 0.000 description 3
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 3
- 238000005137 deposition process Methods 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
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- G—PHYSICS
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- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/02—Optical fibres with cladding with or without a coating
- G02B6/02214—Optical fibres with cladding with or without a coating tailored to obtain the desired dispersion, e.g. dispersion shifted, dispersion flattened
- G02B6/02219—Characterised by the wavelength dispersion properties in the silica low loss window around 1550 nm, i.e. S, C, L and U bands from 1460-1675 nm
- G02B6/02276—Dispersion shifted fibres, i.e. zero dispersion at 1550 nm
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- C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
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- C03B37/012—Manufacture of preforms for drawing fibres or filaments
- C03B37/014—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD]
- C03B37/018—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD] by glass deposition on a glass substrate, e.g. by inside-, modified-, plasma-, or plasma modified- chemical vapour deposition [ICVD, MCVD, PCVD, PMCVD], i.e. by thin layer coating on the inside or outside of a glass tube or on a glass rod
- C03B37/01807—Reactant delivery systems, e.g. reactant deposition burners
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B37/00—Manufacture or treatment of flakes, fibres, or filaments from softened glass, minerals, or slags
- C03B37/01—Manufacture of glass fibres or filaments
- C03B37/012—Manufacture of preforms for drawing fibres or filaments
- C03B37/014—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD]
- C03B37/018—Manufacture of preforms for drawing fibres or filaments made entirely or partially by chemical means, e.g. vapour phase deposition of bulk porous glass either by outside vapour deposition [OVD], or by outside vapour phase oxidation [OVPO] or by vapour axial deposition [VAD] by glass deposition on a glass substrate, e.g. by inside-, modified-, plasma-, or plasma modified- chemical vapour deposition [ICVD, MCVD, PCVD, PMCVD], i.e. by thin layer coating on the inside or outside of a glass tube or on a glass rod
- C03B37/01853—Thermal after-treatment of preforms, e.g. dehydrating, consolidating, sintering
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/02—Optical fibres with cladding with or without a coating
- G02B6/036—Optical fibres with cladding with or without a coating core or cladding comprising multiple layers
- G02B6/03616—Optical fibres characterised both by the number of different refractive index layers around the central core segment, i.e. around the innermost high index core layer, and their relative refractive index difference
- G02B6/03661—Optical fibres characterised both by the number of different refractive index layers around the central core segment, i.e. around the innermost high index core layer, and their relative refractive index difference having 4 layers only
- G02B6/03666—Optical fibres characterised both by the number of different refractive index layers around the central core segment, i.e. around the innermost high index core layer, and their relative refractive index difference having 4 layers only arranged - + - +
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2201/00—Type of glass produced
- C03B2201/06—Doped silica-based glasses
- C03B2201/08—Doped silica-based glasses doped with boron or fluorine or other refractive index decreasing dopant
- C03B2201/12—Doped silica-based glasses doped with boron or fluorine or other refractive index decreasing dopant doped with fluorine
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- C03B2201/20—Doped silica-based glasses doped with non-metals other than boron or fluorine
- C03B2201/28—Doped silica-based glasses doped with non-metals other than boron or fluorine doped with phosphorus
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- C03B2201/30—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
- C03B2201/31—Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with germanium
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- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2203/00—Fibre product details, e.g. structure, shape
- C03B2203/10—Internal structure or shape details
- C03B2203/22—Radial profile of refractive index, composition or softening point
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- C03B2203/36—Dispersion modified fibres, e.g. wavelength or polarisation shifted, flattened or compensating fibres (DSF, DFF, DCF)
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- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B2207/00—Glass deposition burners
- C03B2207/80—Feeding the burner or the burner-heated deposition site
- C03B2207/85—Feeding the burner or the burner-heated deposition site with vapour generated from liquid glass precursors, e.g. directly by heating the liquid
- C03B2207/86—Feeding the burner or the burner-heated deposition site with vapour generated from liquid glass precursors, e.g. directly by heating the liquid by bubbling a gas through the liquid
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Abstract
有平滑环状折射率分布的分散移动光纤的制造方法包括步骤:用外部氧气或氢气燃烧器加热石英管,使温度从1875℃升至1903℃,向石英管供料,沉积第一皮层;在1900℃的恒定温度下,供给原料,沉积环状部分;将温度从1890℃升到1897℃,同时供料,沉积第二皮层;在温度从1920℃降至1890℃的九个过程中加热,沉积芯件部分;和使沉积的光纤在2300-2360℃冷凝,密封。
The method of manufacturing a dispersed moving optical fiber with a smooth annular refractive index profile comprises the steps of: heating the quartz tube with an external oxygen or hydrogen burner to increase the temperature from 1875°C to 1903°C, feeding the quartz tube, depositing the first skin layer; At a constant temperature of 1900°C, feed the raw material to deposit the annular part; raise the temperature from 1890°C to 1897°C, feed the material at the same time, deposit the second skin layer; heat in nine processes from 1920°C to 1890°C, depositing the core part; and condensing the deposited optical fiber at 2300-2360° C., and sealing.
Description
本发明涉及分散移动光导纤维,更详细地说,本发明涉及在芯件周围具有低于芯件的环状折射率分布的分散移动光导纤维及其制造方法,该方法通过将化学气体注入石英管的MCVD方法使折射率平滑并且外部燃烧器加热以便沉积,从而使该光导纤维的几何结构均匀。The present invention relates to dispersed moving optical fibers, and more particularly, the present invention relates to dispersed moving optical fibers having an annular refractive index distribution around a core member lower than that of the core member and a method of manufacturing the same by injecting a chemical gas into a quartz tube The MCVD method smoothes the index of refraction and heats the external burner for deposition, making the geometry of the optical fiber uniform.
本申请基于韩国40089/1995号申请,该申请已被列入本文参考文献。This application is based on Korean Application No. 40089/1995, which is incorporated herein by reference.
近来分散移动光导纤维(将1.55μm的石英光导纤维用于高速信息网络)的品种及性能均有变化。分散移动光导纤维的品种和性能在参考文献(“OPTICAL FIBER TELECOMMUNICATIONII”published in Academic Press,Inc.,Pages 29-36)中已作详细叙述,本说明书将它省去。不分散移动光导纤维,尤其是,具有环状折射率分布的分散移动光导纤维是众所周知的,因为它具有良好的微弯曲损失。这种结构的光导纤维是由Mr.Bhagavatula和他的同事在1983年提出的,分别公开在US4412722(1983)和US4516826(1984)中,据报道,它在芯件周围有一层用来保护芯件的低环状折射率。它主要是用OVD(外汽相沉积法)和MCVD(改进的化学汽相沉积法)制造的。即,通过OVD难以制造具有阶梯式的环状折射率分布结构(公开在US4715679、KR26410和KR49509中)的光导纤维,尽管它易于制造具有三角形环状分布结构的光导纤维,或也易于制造基料外径相对大到某种程度的多孔结构。然而,MCVD由于通过内沉积来均匀控制流量,使它易于制造任何所要分布的光导纤维(如US4737179,US4755022和US4822399所述),但它不能制造基料具有大外径的光导纤维。Recently, the variety and performance of dispersed mobile optical fibers (using 1.55 μm quartz optical fibers for high-speed information networks) have changed. The variety and performance of the dispersed mobile optical fiber have been described in detail in the reference ("OPTICAL FIBER TELECOMMUNICATION II" published in Academic Press, Inc., Pages 29-36), and this specification will omit it. Non-dispersive migrating optical fibers, in particular, dispersive migrating optical fibers with annular refractive index profiles are well known because of their good microbending losses. The optical fiber of this structure was proposed by Mr.Bhagavatula and his colleagues in 1983, disclosed in US4412722 (1983) and US4516826 (1984) respectively, it is reported that it has a layer around the core to protect the core low ring refractive index. It is mainly manufactured by OVD (Outside Vapor Deposition) and MCVD (Modified Chemical Vapor Deposition). That is, it is difficult to manufacture an optical fiber having a stepped annular refractive index distribution structure (disclosed in US4715679, KR26410, and KR49509) by OVD, although it is easy to manufacture an optical fiber having a triangular annular distribution structure, or it is also easy to manufacture a base A porous structure with a relatively large outer diameter to some extent. However, MCVD makes it easy to manufacture optical fibers of any desired distribution due to uniform flow control by in-deposition (as described in US4737179, US4755022 and US4822399), but it cannot produce optical fibers with a base material having a large outer diameter.
参照图1系统,图2和图3的现有技术说明将恒定量的原料气体从原料气体供给系统供给用燃烧器加热至恒定温度的石英管,结果可制造具有环状折射率分布的分散移动光导纤维。若要更详细的说明上述制造方法,则在沉积第一皮层前,光在指定时间内加热石英管,使石英管的表面温度达到1890℃,从而使石英管内部均匀,再用外部氧气或氢气燃烧器在1890℃继续加热,同时供给5400mg/分的SiCl4、450mg/分GeCl4、40mg/分POCl3和12cc/分CF4(如图3B-3F所示)。此后,向石英管内供入3000mg/分SiCl4、1300mg/分 GeCl4、35mg/分 POCl3和2000cc/分O2,均匀加热至不超过1905℃以便沉积环状部分,如图3A所示。然后,向石英管供入4000mg/分SiCl4、450mg/分GeCl4、25mg/分POCl3和9cc/分CF4,均匀加热至1915℃以便生成第二皮层(如图3A所示)。除此以外,向石英管供入1100mg/分SiCl4和2000mg/分O2,加入GeCl4使之不超过60-250mg/分,同时在1910℃均匀加热该管,以便沉积芯件部分。将在石英管中沉积完成的光导纤维在2300-2320℃冷凝,将30-40cc/分的CF4加到已冷凝的光导纤维中。最后,在2220-2250℃将其蚀刻,加热到2340-2360℃,使其紧密密封和封闭,如图3A所示。Referring to the system of Figure 1, the prior art of Figures 2 and 3 illustrate that a constant amount of raw gas is fed from the raw gas supply system to a quartz tube heated to a constant temperature by a burner, resulting in the manufacture of dispersed moving Optical fiber. To explain the above manufacturing method in more detail, before depositing the first skin layer, the light heats the quartz tube for a specified time, so that the surface temperature of the quartz tube reaches 1890 ° C, so that the inside of the quartz tube is uniform, and then the external oxygen or hydrogen is used to The burner continued heating at 1890°C while supplying 5400mg/min of SiCl 4 , 450mg/min of GeCl 4 , 40mg/min of POCl 3 and 12cc/min of CF 4 (as shown in Figures 3B-3F). Thereafter, 3000 mg/min of SiCl4 , 1300 mg/min of GeCl4 , 35 mg/min of POCl3 and 2000 cc/min of O2 were supplied into the quartz tube and uniformly heated to not more than 1905°C to deposit the annular portion, as shown in Fig. 3A. Then, 4000 mg/min SiCl 4 , 450 mg/min GeCl 4 , 25 mg/min POCl 3 and 9 cc/min CF 4 were fed into the quartz tube and uniformly heated to 1915° C. to form the second skin layer (as shown in FIG. 3A ). Besides, 1100 mg/min of SiCl4 and 2000 mg/min of O2 were fed into the quartz tube, and GeCl4 was added so as not to exceed 60-250 mg/min while uniformly heating the tube at 1910C to deposit the core part. The optical fiber deposited in the quartz tube was condensed at 2300-2320°C, and 30-40cc/min of CF4 was added to the condensed optical fiber. Finally, it is etched at 2220-2250°C and heated to 2340-2360°C to make it tightly sealed and closed, as shown in Figure 3A.
上述现有技术具有环状分布的分散移动光导纤维其芯件具有圆锥形折射率。对于芯件中心的最大折射率而言,GeO2的量必须增加直到芯件中心。然而,在MCVD方法中,在GeO2增加过程中,会导致中心下降问题,即在沉积过程中和在芯件中心出现折射率减小现象。The prior art described above has an annular distribution of dispersed moving optical fibers whose core members have a conical refractive index. For the maximum refractive index at the center of the core, the amount of GeO2 must be increased up to the center of the core. However, in the MCVD method, during the GeO2 addition, it causes a center drop problem, that is, a decrease in the refractive index occurs during the deposition process and at the center of the core.
上述光导纤维还有另一个问题,当基料得自光导纤维时,由于与普通单模光导纤维相比芯件直径小,所以沿光导纤维中基料的长度方向,光学性能偏差很大。The above-mentioned optical fiber has another problem in that when the base material is obtained from the optical fiber, since the diameter of the core member is small compared with the ordinary single-mode optical fiber, the optical properties deviate greatly along the length of the base material in the optical fiber.
本发明一个目的是通过调节基料沉淀过程中的沉积温度和沉积进料流量,并通过向GeO2中加入给定量的SF6和CF4,(GeO2在基料制造过程中在高温下会在芯件中心挥发)以减少中心下降,从而提供导致非波形折射率的方法。One object of the present invention is by adjusting the deposition temperature and the deposition feed flow in the base material precipitation process, and by adding a given amount of SF 6 and CF 4 in GeO 2 Volatilize at the center of the wick) to reduce center dip, thereby providing a means of causing a non-waveform refractive index.
本发明另一个目的是通过增加基料外径而提供使芯件直径均匀的方法。Another object of the present invention is to provide a method of making the diameter of the core member uniform by increasing the outer diameter of the base material.
按照本发明,具有平滑环状折射率分布的分散移动光导纤维的制造方法包括下列步骤:(a)用外部氧气或氢气燃烧器加热石英管,使其温度从1875℃提高到1903℃,向石英管供给原料,包括5200mg/分SiCl4、430mg/分 GeCl4、30mg/分 POCl3和9CC/分CF4,以沉积第一皮层;(b)在1900℃的恒定温度下,供给原料,包括3300mg/分SiCl4、1150mg/分GeCl4、20mg/分POCl3和1500cc/分O2以沉积环状部分;(c)将温度从1890℃提高到1897℃,同时供给原料,包括3800mg/分SiCl4、430mg/分GeCl4、10mg/分POCl3和7cc/分CF4以沉积第二皮层;(d)在温度从1920℃降至1890℃的九个降温过程中进行加热,以沉积芯件部分,在该九个过程中SiCl4的进料流量从380mg/分减为260mg/分,在该九个过程中GeCl4的进料流量从20mg/分增至195mg/分,在该九个过程中,O2进料流量保持1500cc/分不变;和(e)使完成沉积的光导纤维在2300-2360℃冷凝,将30-40cc/分CF4加入石英管中,在2220-2250℃蚀刻,并在2350-2370℃向石英管中加入100cc/分Cl2以便密封和封闭。According to the present invention, the manufacturing method of the dispersed moving optical fiber with smooth annular refractive index distribution comprises the following steps: (a) heating the quartz tube with an external oxygen or hydrogen burner to increase its temperature from 1875°C to 1903°C, Tube supply raw materials, including 5200mg/min SiCl 4 , 430mg/min GeCl 4 , 30mg/min POCl 3 and 9CC/min CF 4 , to deposit the first skin layer; (b) at a constant temperature of 1900°C, supply raw materials including 3300 mg/min SiCl 4 , 1150 mg/min GeCl 4 , 20 mg/min POCl 3 and 1500 cc/min O 2 to deposit the annular part; (c) increase the temperature from 1890°C to 1897°C while supplying raw materials including 3800mg/min SiCl 4 , 430 mg/min GeCl 4 , 10 mg/min POCl 3 and 7 cc/min CF 4 to deposit the second skin layer; (d) heating during nine ramps from 1920°C to 1890°C to deposit the core Parts, in these nine processes, the feed flow of SiCl 4 is reduced from 380mg/min to 260mg/min, and in these nine processes, the feed flow of GeCl 4 is increased from 20mg/min to 195mg/min, and in these nine processes During this process, the O feed flow rate remains constant at 1500cc/min; and (e) condenses the deposited optical fiber at 2300-2360°C, and 30-40cc/ min CF is added to the quartz tube at 2220-2250°C. ℃ etching, and add 100cc/min Cl 2 to the quartz tube at 2350-2370℃ to seal and seal.
图1是普通MCVD制造方法的示意图;Fig. 1 is the schematic diagram of common MCVD manufacturing method;
图2是现有技术的环状分布;Fig. 2 is the circular distribution of prior art;
图3A表示常规环状分布的制造方法中各个过程的加热温度;Fig. 3 A represents the heating temperature of each process in the manufacturing method of conventional annular distribution;
图3B表示常规环状分布的制造方法中供给各个过程的SiCl4进料流量;Fig. 3 B represents the SiCl of supplying each process in the manufacturing method of conventional annular distribution Feed flow rate;
图3C表示常规环状分布的制造方法中供给各个过程的GeCl4的进料流量;Fig. 3 C represents the feed flow rate of GeCl supplied to each process in the manufacturing method of conventional annular distribution;
图3D表示常规环状分布制造方法中供给各个过程的POCl3进料流量;Figure 3D represents the POCl3 feed flow rate supplied to each process in a conventional annular distribution manufacturing process;
图3E表示常规环状分布制造方法中供给各个过程的O2进料流量;Figure 3E represents the O feed flow rates supplied to each process in a conventional annular distribution manufacturing process;
图3F表示常规环状分布制造方法中供给各个过程的CF4(SF6)进料流量;Figure 3F represents the CF4 ( SF6 ) feed flow rate for each process in a conventional annular distribution manufacturing process;
图4是本发明的环状分布;Fig. 4 is the annular distribution of the present invention;
图5A表示按本发明的平滑环状折射率分布制造方法中各个过程的加热温度;Fig. 5 A shows the heating temperature of each process in the manufacturing method of the smooth annular refractive index distribution according to the present invention;
图5B表示按本发明的平滑环状折射率分布制造方法中供给各个过程的SiCl4进料流量;Fig. 5 B represents the SiCl feed flow rate supplied to each process in the smooth annular refractive index profile manufacturing method of the present invention;
图5C表示按本发明的平滑环状折射率分布制造方法中供给各个过程的GeCl4进料流量;Fig. 5 C shows the GeCl feed flow rate supplied to each process in the smooth annular refractive index profile manufacturing method of the present invention;
图5D表示按本发明的平滑环状折射率分布制造方法中供给各个过程的POCl3进料流量;Figure 5D shows the POCl3 feed flow rate supplied to each process in the smooth annular refractive index profile manufacturing method of the present invention;
图5E表示按本发明的平滑环状折射率分布制造方法中供给各个过程的O2进料流量;Figure 5E shows the O feed flow rates supplied to each process in the smooth annular refractive index profile manufacturing method of the present invention;
图5F表示按本发明的平滑环状折射率分布制造方法中供给各个过程的CF4(SF6)进料流量;和Fig. 5F shows the feed flow rate of CF 4 (SF 6 ) supplied to each process in the smooth annular refractive index profile manufacturing method according to the present invention; and
图5G表示按本发明的平滑环状折射率分布制造方法中供给各个过程的Cl2进料流量。FIG. 5G shows the Cl2 feed flow rate to each process in the smooth annular refractive index profile manufacturing method according to the present invention.
图1说明在恒定温度下用燃烧器加热石英管时,使指定量的原料气体通过原料气体供应器供给石英管,从而制造具有环状折射率的分散移动光导纤维。上述方法详述如下:加热石英管直至其表面温度为1875℃,并保持一定时间,致使其内表面温度均匀,如图5A所示。然后,如图5B-5G所示,再用外部氧气或氢气燃烧器加热石英管,使其温度从在九个过程中1875℃升至1903℃,温度提高3.5℃,同时,供给5200mg/分SiCl4、430mg/分GeCl4、30mg/分POCl3和9cc/分CF4以便沉积第一皮层。为沉积环状部分,如图5A所示,在1900℃的恒定沉积温度下供给3300mg/分SiCl4、1150mg/分GeCl4、20mg/分POCl3和1500cc/分的O2。接着,为了制备第二皮层,向石英管内供给原料,包括3800mg/分SiCl4、430mg/分GeCl4、10mg/分POCl3和7cc/分CF4(如图5B-5G所示),同时使温度从1890℃提高到1897℃(如图5A所示)。最后,在图5A的九个过程中,使沉积温度从1920℃降至1890℃,以沉积芯件部分。同时,在九个过程中将SiCl4进料流量从380mg/分降至260mg/分,在九个过程中GeCl4进料流量从20mg/分增加到195mg/分,在九个过程中O2进料流量保持1500cc/分不变。为此,原料进料流量示于表1中。Fig. 1 illustrates that while a quartz tube is heated by a burner at a constant temperature, a specified amount of raw material gas is supplied to the quartz tube through a raw material gas supplier to manufacture a dispersed moving optical fiber having a ring-shaped refractive index. The above method is described in detail as follows: the quartz tube is heated until its surface temperature is 1875° C., and maintained for a certain period of time, so that the inner surface temperature is uniform, as shown in FIG. 5A . Then, as shown in Figure 5B-5G, the quartz tube was heated with an external oxygen or hydrogen burner, and its temperature was increased from 1875 ° C to 1903 ° C in nine processes, and the temperature was increased by 3.5 ° C. At the same time, 5200 mg/min SiCl was supplied 4. 430 mg/min GeCl 4 , 30 mg/min POCl 3 and 9 cc/min CF 4 to deposit the first skin layer. To deposit the annular portion, as shown in Figure 5A, 3300 mg/min SiCl4 , 1150 mg/min GeCl4, 20 mg/min POCl3 and 1500 cc/min O2 were supplied at a constant deposition temperature of 1900°C. Next, in order to prepare the second skin layer, supply raw materials into the quartz tube, including 3800mg/min SiCl 4 , 430mg/min GeCl 4 , 10mg/min POCl 3 and 7cc/min CF 4 (as shown in Figures 5B-5G), while making The temperature was increased from 1890°C to 1897°C (as shown in Figure 5A). Finally, in the nine passes of Figure 5A, the deposition temperature was lowered from 1920°C to 1890°C to deposit the core portion. Simultaneously, the feed flow rate of SiCl 4 was reduced from 380 mg/min to 260 mg/min in nine processes, the feed flow rate of GeCl 4 was increased from 20 mg/min to 195 mg/min in nine processes, and O 2 in nine processes The feed flow was kept constant at 1500 cc/min. For this purpose, the raw material feed flows are shown in Table 1.
表1
然后,使沉积好的光导纤维如图5A所示在2300-2360℃冷凝,将30-40cc/分的CF4加入石英管中(如图5F所示)。在2220-2250℃蚀刻后,将100cc/分Cl2供给石英管(如图5G所示),同时在2350-2370℃加热(如图5A所示)以便密封和封闭。Then, the deposited optical fiber was condensed at 2300-2360° C. as shown in FIG. 5A , and 30-40 cc/min of CF 4 was added into the quartz tube (as shown in FIG. 5F ). After etching at 2220-2250°C, 100cc/min Cl2 was supplied to the quartz tube (as shown in Figure 5G) while heating at 2350-2370°C (as shown in Figure 5A) to seal and seal.
在本发明的另一个实施方案中,使九个过程中沉积温度从1905℃降至1890℃以沉积芯件部分。同时,使九个过程中SiCl4进料流量从300mg/分降至260mg/分,使九个过程中GeCl4进料流量从20mg/分增加到195mg/分,使九个过程中O2进料流量保持1500cc/分不变。为此,原料进料流量示于表2中。In another embodiment of the present invention, the deposition temperature was reduced from 1905°C to 1890°C in nine passes to deposit core portions. At the same time, the feed flow rate of SiCl4 in the nine processes is reduced from 300mg/min to 260mg/min, the feed flow rate of GeCl4 in the nine processes is increased from 20mg/min to 195mg/min, and the flow rate of O2 in the nine processes is increased. The material flow remains constant at 1500cc/min. For this purpose, the raw material feed flows are shown in Table 2.
表2
在一发明又一个实施方案中,使九个过程中沉积温度从1905℃降至1890℃,以沉积芯件部分。同时,使九个过程中SiCl4进料流量从300mg/分降至260mg/分,九个过程中GeCl4进料流量从30mg/分增加到195mg/分,九个过程中O2进料流量保持1500ccm/分不变。为此,原料进料流量示于表3中。In yet another embodiment of an invention, the deposition temperature was reduced from 1905°C to 1890°C in nine passes to deposit core portions. At the same time, the feed flow rate of SiCl4 in the nine processes was reduced from 300mg/min to 260mg/min, the feed flow rate of GeCl4 in the nine processes was increased from 30mg/min to 195mg/min, and the feed flow rate of O2 in the nine processes was Keep 1500ccm/min unchanged. For this purpose, the raw material feed flows are shown in Table 3.
表3
如上所述,本发明通过调节基料沉积过程中的沉积温度和沉积进料流量,并向GeO2中加入指定量的SF6和CF4,(GeO2在基料密封和封闭过程中在高温下在芯件中心挥发)以减少中心下降,从而提供导致非波形折射率的方法。另外,本发明通过外包层方法使基料外径增加,从而提供使芯件直径均匀的方法。因此,本发明优点是它使光导纤维的损耗得以改进,并具有很稳定的色分散性能。As mentioned above, the present invention is by adjusting the deposition temperature and the deposition feed flow rate in the base material deposition process, and adds the specified amount of SF 6 and CF 4 in GeO 2 , (GeO 2 is at high temperature in the base material sealing and sealing process volatilization at the center of the wick) to reduce the center drop, thereby providing a means of causing a non-waveform refractive index. In addition, the present invention provides a method of making the diameter of the core member uniform by increasing the outer diameter of the base material by the overcladding method. Therefore, the present invention is advantageous in that it enables improved optical fiber loss and has very stable color dispersion properties.
因此,应该明白,本发明不限于本文所公开的作为完成本发明最佳方式的特定实施方案,也可以说,本发明不限于本说明书中所述的具体实施方案,除了所附权利要求中所限定的以外。Therefore, it should be understood that this invention is not limited to the particular embodiment disclosed herein as the best mode for carrying out this invention, nor is it limited to the particular embodiment described in this specification except as described in the appended claims. beyond the limits.
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KR1019950040089A KR0153835B1 (en) | 1995-11-07 | 1995-11-07 | Process for preparation of optical glass fiber |
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AUPQ935500A0 (en) * | 2000-08-11 | 2000-09-07 | Jds Uniphase Pty Ltd | Optical waveguide with minimised cladding mode coupling |
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US6483975B1 (en) * | 2001-04-27 | 2002-11-19 | Fitel Usa Corp. | Positive dispersion optical fiber having large effective area |
US6807350B2 (en) * | 2001-07-17 | 2004-10-19 | Verrillon, Inc. | Optical fiber with a radially varying index of refraction and related methods |
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JP2004307280A (en) * | 2003-04-08 | 2004-11-04 | Shin Etsu Chem Co Ltd | Glass preform for optical fiber in which absorption due to hydroxide group is reduced and a method of manufacturing the same |
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